Investigating Brain Function in People With and Without Visual Snow Syndrome Using Adaptation to Visual Stimuli

NCT06961864 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2026-01-14

No results posted yet for this study

Summary

The goal of this study is to learn more about the brain pathways and activity involved in creating Visual Snow Syndrome (VSS). The main questions it aims to answer are:

* Does VSS arise from spontaneous activity in brain pathways?
* Where in the brain does the activity contributing to VSS arise?
* How does brain activity contribute to VSS?

Participants will:

1. Undergo assessments and questionnaires to understand visual and mental symptoms, cognitive, and sensory function.
2. Make visual judgements based on images presented to them both inside and outside a magnetic resonance imaging (MRI) machine.
3. Undergo scanning of their brain while inside of an MRI machine.

Conditions

Interventions

BEHAVIORAL

Visual Adaptation

Presentation of visual stimuli to quantify the appearance of visual snow or its effects in the visual system of the brain.

BEHAVIORAL

Assessments and Questionnaires

Administration of clinical assessments and questionnaires to gather information about visual and mental symptoms, cognitive, and sensory function.

DEVICE

Functional Magnetic Resonance Imaging (fMRI)

7 tesla fMRI data will be acquired during visual paradigms designed to measure neural responses with and without adaptation.

DEVICE

Magnetic Resonance Imaging (MRS)

7 tesla MRS data will be acquired to quantify the concentrations of different brain chemicals in brain regions including visual cortex.

Sponsors & Collaborators

Principal Investigators

  • Michael-Paul Schallmo, Ph.D. · University of Minnesota, Department of Psychiatry and Behavioral Sciences

  • Stephen A Engel, Ph.D. · University of Minnesota, Department of Psychology

  • Michael S Lee, M.D. · University of Minnesota, Department of Ophthalmology and Visual Neurosciences

  • Abby Metzler, M.D. · University of Minnesota, Department of Neurology

  • Malgorzata Marjanska, Ph.D. · University of Minnesota, Department of Radiology

  • Carrie E Robertson, M.D. · Mayo Clinic, Rochester, Department of Neurology

Study Design

Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-04-11
Primary Completion
2030-03-31
Completion
2030-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06961864 on ClinicalTrials.gov